ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3652-12T>A

dbSNP: rs1378688228
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001184053 SCV001349925 likely benign Familial thoracic aortic aneurysm and aortic dissection 2019-01-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003514480 SCV004281591 likely benign Aortic aneurysm, familial thoracic 4 2023-12-22 criteria provided, single submitter clinical testing

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